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BMC Genetics 2011
Genome-wide linkage study of atopic dermatitis in West Highland White TerriersAbstract: Blood samples and health questionnaires were collected from 108 WHWTs spanning three families. A linkage simulation using these 108 dogs showed high power to detect a highly penetrant mutation. Ninety WHWTs were genotyped using markers from the Minimal Screening Set 2 (MSS-2). Two hundred and fifty six markers were informative and were used for linkage analysis. Using a LOD score of 2.7 as a significance threshold, no chromosomal regions were identified with significant linkage to AD. LOD scores greater than 1.0 were located in a 56 cM region of chromosome 7.The study was unable to detect any chromosomal regions significantly linked to canine AD. This could be a result of factors such as environmental modification of phenotype, incorrect assignment of phenotype, a mutation of low penetrance, or incomplete genome coverage. A genome-wide SNP association study in a larger cohort of WHWTs may prove more successful by providing higher density coverage and higher statistical power.Canine atopic dermatitis (AD) is a common, heritable, chronic allergic skin condition that can cause lifelong morbidity in dogs [1,2]. AD is the ninth most common disorder diagnosed in veterinary practice [3], and certain dog breeds such as the West Highland White Terrier (WHWT), with a prevalence as high as 18.7% [4], are more susceptible to the condition than others [5]. In canine AD, environmental allergens such as house dust mites [6] trigger an inflammatory response leading to the development of erythematous macules and papular lesions [7]. Clinical signs usually manifest between six months and three years of age and the chronic pruritus associated with AD leads to excessive licking, alopecia, hyperpigmentation, scaling, lichenification and secondary bacterial and yeast infections [8]. Diagnosis is based on a set of general criteria including chronic or chronic-relapsing pruritus and dermatitis, classical appearance and distribution of lesions, and family history or breed predisposition and
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